COC1OC2COC(OC2C(OC(=O)C2=CC(OC)=C(OC)C(OC)=C2)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1)C1=CC=CC=C1

InChIKey=YSDMESBIEUSJBT-UHFFFAOYSA-N

C34H38O14

670.664

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Gallic acid and derivatives P-methoxybenzoic acids and derivatives M-methoxybenzoic acids and derivatives Pyranodioxins Benzoic acid esters Phenoxy compounds Methoxybenzenes Anisoles Benzoyl derivatives Alkyl aryl ethers Oxanes 1,3-dioxanes Monosaccharides Dicarboxylic acids and derivatives Carboxylic acid esters Acetals Oxacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Gallic acid or derivatives - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Benzoate ester - Pyranodioxin - Benzoic acid or derivatives - Methoxybenzene - Anisole - Phenol ether - Benzoyl - Phenoxy compound - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Meta-dioxane - Oxane - Dicarboxylic acid or derivatives - Monosaccharide - Carboxylic acid ester - Carboxylic acid derivative - Acetal - Oxacycle - Ether - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Not available